Evidence map›Paper›PMID 12353912›Full record

ArticleMolecular biotechnology2002

Functional cloning using pFB retroviral cDNA expression libraries.

Katherine A Felts, Keith Chen, Kim Zaharee, Latha Sundar, Jamie Limjoco, Anna Miller, Peter Vaillancourt

Abstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Molecular biotechnology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Katherine A FeltsApplied Molecular Evolution, San Diego, California 92121, USA.
Keith Chen
Kim Zaharee
Latha Sundar
Jamie Limjoco
Anna Miller
Peter Vaillancourt

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retroviral cDNA expression libraries allow the efficient introduction of complex cDNA libraries into virtually any mitotic cell type for screening based on gene function. The cDNA copy number per cell can be easily controlled by adjusting the multiplicity of infection, thus cell populations may be generated in which >90% of infected cells contain one to three cDNAs. We describe the isolation of two known oncogenes and one cell-surface receptor from a human Burkitt's lymphoma (Daudi) cDNA library inserted into the high-titer retroviral vector pFB.

Indexed as

Cell Cycle ProteinsGene LibraryGenetic Vectors3T3 CellsAnimalsBase SequenceBurkitt LymphomaCloning, MolecularDNA, ComplementaryGene Expression ProfilingGene Expression RegulationHumansMiceMolecular Sequence DataOncogenesProto-Oncogene ProteinsCell Cycle ProteinsDNA, ComplementaryProto-Oncogene ProteinsProto-Oncogene Proteins c-rafProto-Oncogene Proteins c-vavReceptors, Interleukin-4Recombinant ProteinsVAV1 protein, humanVav1 protein, mouse

Identifiers

PMID12353912

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.